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4. Congenital myopia in Stickler's hereditary arthro-ophthalmopathy. Wang FM; Afran SI; Goldberg RB Am J Ophthalmol; 1990 Oct; 110(4):435-6. PubMed ID: 2220987 [No Abstract] [Full Text] [Related]
5. Stickler's syndrome. A report of a family. Hill JC; Nelson MM S Afr Med J; 1989 Mar; 75(5):238-41. PubMed ID: 2928863 [TBL] [Abstract][Full Text] [Related]
18. A-2-->G transition at the 3' acceptor splice site of IVS17 characterizes the COL2A1 gene mutation in the original Stickler syndrome kindred. Williams CJ; Ganguly A; Considine E; McCarron S; Prockop DJ; Walsh-Vockley C; Michels VV Am J Med Genet; 1996 Jun; 63(3):461-7. PubMed ID: 8737653 [TBL] [Abstract][Full Text] [Related]
20. Hearing loss in Stickler's syndrome: a family case study. Jacobson J; Jacobson C; Gibson W J Am Acad Audiol; 1990 Jan; 1(1):37-40. PubMed ID: 2132580 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]